TRIACTING DAY TIME WITH PE- dextromethorphan hydrobromide, phenylephrine hydrochloride liquid 
AmerisourceBergen Drug Corporation (Good Neighbor Pharmacy) 24385

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients

Dextromethorphan HBr, USP 5 mg
Phenylephrine HCI, USP 2.5 mg

Purposes

Dextromethorphan HBr, USP............Cough suppressant
Phenylephrine HCI, USP...................Nasal decongestant

Uses

temporarily relieves:
• nasal and sinus congestion
• cough due to minor throat and bronchial irritation
associated with the common coldEnter section text here

Warnings

Do Not Use

• in a child under 4 years of age
• in a child who is taking a prescription monoamine
oxidase inhibitor (MAOI) (certain drugs for depression,
psychiatric or emotional conditions, or Parkinson’s
disease), or for 2 weeks after stopping the MAOI drug.
If you do not know if your child's prescription drug
contains an MAOI, ask a doctor or pharmacist before
giving this product.

Ask a doctor before use if the child has

• heart disease • high blood pressure
• thyroid disease • diabetes
• a breathing problem such as chronic bronchitis
• cough that occurs with too much phlegm (mucus)
or chronic cough that lasts
• do not give this product for persistent or chronic cough
such as occurs with asthma or if cough is accompanied
by excessive phlegm (mucus) unless directed by a doctor

When using this product

• do not exceed recommended dosage

Stop use and ask a doctor if

• nervousness, dizziness or sleeplessness occurs
• symptoms do not improve within 7 days or occur
with a fever
• cough persists for more than 7 days, comes back
or occurs with fever, rash or persistent headache.
These could be signs of a serious condition.

Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek
professional assistance or contact a Poison Control
Center immediately.

Directions

• take every 4 hours; not to exceed
6 doses in 24 hours or as directed by a doctor

age                                                             dose
children 6 years to under 12 years        2 teaspoonfuls (tsps)
children 4 years to under 6 years          1 teaspoonful (tsp)
children under 4 years                            do not use

Other Information

each teaspoon contains: sodium 2 mg
• contains no aspirin
• store at controlled room temperature

Inactive Ingredients

acesulfame potassium,
benzoic acid, citric acid, edetate disodium, flavors,
maltitol solution, propylene glycol, purified water,
red 40, sodium citrate

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Compare to active ingredients in Triaminic® Day Time Cold and Cough*

Cherry Flavor

Children's

Triacting

Day Time Cold and Cough

4 FL OZ (118 mL)

image of label


TRIACTING DAY TIME  WITH PE
dextromethorphan hydrobromide, phenylephrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-148
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE5 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE2.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
MALTITOL (UNII: D65DG142WK)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (Cherry Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24385-148-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/20/200903/31/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34107/20/200903/31/2017
Labeler - AmerisourceBergen Drug Corporation (Good Neighbor Pharmacy) 24385 (007914906)

Revised: 6/2017
 
AmerisourceBergen Drug Corporation (Good Neighbor Pharmacy) 24385